Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance.
- NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_assertion wasGeneratedBy ECO_0000203 NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance.
- NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_assertion wasDerivedFrom befree-20150227 NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance.
- NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_assertion SIO_000772 19473076 NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance.
- NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_assertion evidence source_evidence_literature NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance.
- NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_assertion description "[Congenital contractural arachnodactyly (Beals syndrome) is a rare autosomal dominantly inherited connective tissue disorder characterized by flexion contractures, arachnodactyly, crumpled ears, and mild muscular hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396115.RAIKwuPSlUJBtPK9H0aEWDAur2NF_j5oyY5EFpa2h51wY130_provenance.